Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g11680 A10 13267992 G A upstream_gene_variant MODIFIER c.-4230G>A| S35
2 BAA10g11680 A10 13268608 G A upstream_gene_variant MODIFIER c.-3614G>A| S274
3 BAA10g11680 A10 13268856 C T upstream_gene_variant MODIFIER c.-3366C>T| S282
4 BAA10g11680 A10 13272661 C T missense_variant MODERATE c.440C>T|p.Pro147Leu S259
5 BAA10g11680 A10 13272861 C T stop_gained HIGH c.640C>T|p.Arg214* S235
6 BAA10g11680 A10 13272948 G A missense_variant MODERATE c.727G>A|p.Ala243Thr S202
7 BAA10g11680 A10 13273081 G A missense_variant MODERATE c.860G>A|p.Arg287Lys S283
8 BAA10g11680 A10 13273136 G A synonymous_variant LOW c.915G>A|p.Lys305Lys S274
9 BAA10g11680 A10 13273849 C T missense_variant MODERATE c.1454C>T|p.Pro485Leu S23
10 BAA10g11680 A10 13273889 C T synonymous_variant LOW c.1494C>T|p.Ser498Ser S249
11 BAA10g11680 A10 13273903 G A missense_variant MODERATE c.1508G>A|p.Cys503Tyr S290
12 BAA10g11680 A10 13274453 C T synonymous_variant LOW c.1848C>T|p.Asp616Asp S193
13 BAA10g11680 A10 13274928 C T missense_variant MODERATE c.2323C>T|p.Pro775Ser S162
S169
14 BAA10g11680 A10 13275521 C T missense_variant MODERATE c.2809C>T|p.Pro937Ser S190
15 BAA10g11680 A10 13277401 C T intron_variant MODIFIER c.3154-447C>T| S260
16 BAA10g11680 A10 13277652 C T intron_variant MODIFIER c.3154-196C>T| S237
17 BAA10g11680 A10 13277817 C T intron_variant MODIFIER c.3154-31C>T| S56
18 BAA10g11680 A10 13277821 C T intron_variant MODIFIER c.3154-27C>T| S177
19 BAA10g11680 A10 13278652 G A downstream_gene_variant MODIFIER c.*673G>A| S136
20 BAA10g11680 A10 13278696 C T downstream_gene_variant MODIFIER c.*717C>T| S195
21 BAA10g11680 A10 13278991 C T downstream_gene_variant MODIFIER c.*1012C>T| S162
22 BAA10g11680 A10 13279198 C T downstream_gene_variant MODIFIER c.*1219C>T| S103
23 BAA10g11680 A10 13279242 C T downstream_gene_variant MODIFIER c.*1263C>T| S194
24 BAA10g11680 A10 13279314 G A downstream_gene_variant MODIFIER c.*1335G>A| S55
25 BAA10g11680 A10 13279474 C T downstream_gene_variant MODIFIER c.*1495C>T| S168